Single and Combined Prothrombotic Factors in Patients With Idiopathic Venous Thromboembolism
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References (50)
A simple salting out procedure for extracting DNA from human nucleated cells
1988 • 20,341 citations
Mutation in blood coagulation factor V associated with resistance to activated protein C
1994 • 3,871 citations
A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
1996 • 3,124 citations
Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C.
1993 • 1,997 citations
Relation Between Folate Status, a Common Mutation in Methylenetetrahydrofolate Reductase, and Plasma Homocysteine Concentrations
1996 • 1,423 citations
Venous thrombosis due to poor anticoagulant response to activated protein C: Leiden Thrombophilia Study
1993 • 1,283 citations
World distribution of factor V Leiden
1995 • 1,184 citations
Resistance to Activated Protein C as a Basis for Venous Thrombosis
1994 • 1,148 citations
Role of clotting factor VIII in effect of von Willebrand factor on occurrence of deep-vein thrombosis
1995 • 1,117 citations
Increased risk of venous thrombosis in oral-contraceptive users who are carriers of factor V Leiden mutation
1994 • 1,065 citations
Mutation in the Gene Coding for Coagulation Factor V and the Risk of Myocardial Infarction, Stroke, and Venous Thrombosis in Apparently Healthy Men
1995 • 1,060 citations
High risk of thrombosis in patients homozygous for factor V Leiden (activated protein C resistance) [see comments]
1995 • 1,036 citations
Hyperhomocysteinemia as a Risk Factor for Deep-Vein Thrombosis
1996 • 1,034 citations
Geographic Distribution of the 20210 G to A Prothrombin Variant
1998 • 707 citations
Inherited Thrombophilia: Part 1
1996 • 600 citations
Deficiencies of Coagulation-Inhibiting and Fibrinolytic Proteins in Outpatients with Deep-Vein Thrombosis
1990 • 456 citations
Activated protein C resistance as an additional risk factor for thrombosis in protein C-deficient families
1994 • 446 citations
Familial Dysfibrinogenemia and Thrombophilia
1995 • 326 citations
Resistance to activated protein C as an additional genetic risk factor in hereditary deficiency of protein S
1995 • 314 citations
The Mutation Ala677→Val in the Methylene Tetrahydrofolate Reductase Gene: A Risk Factor for Arterial Disease and Venous Thrombosis
1997 • 313 citations
Coexistence of Hereditary Homocystinuria and Factor V Leiden — Effect on Thrombosis
1996 • 266 citations
The 20210 A Allele of the Prothrombin Gene Is a Common Risk Factor among Swedish Outpatients with Verified Deep Venous Thrombosis
1997 • 255 citations
High prevalence of hyperhomocyst(e)inemia in patients with juvenile venous thrombosis.
1994 • 251 citations
Factor V Leiden (FV R506Q) in Families with Inherited Antithrombin Deficiency
1996 • 237 citations
A Single Genetic Origin for a Common Caucasian Risk Factor for Venous Thrombosis
1997 • 236 citations
The Incidence of Venous Thromboembolism in Family Members of Patients with Factor V Leiden Mutation and Venous Thrombosis
1998 • 207 citations
Thrombophilia as a Multigenic Disorder
1997 • 204 citations
Detection and Quantitative Evaluation of Lupus Circulating Anticoagulant Activity
1987 • 183 citations
Co-inheritance of the 20210A Allele of the Prothrombin Gene Increases the Risk of Thrombosis in Subjects with Familial Thrombophilia
1997 • 177 citations
Prevalence of the Prothrombin Gene Variant (nt20210A) in Venous Thrombosis and Arterial Disease
1997 • 175 citations
The prothrombin gene G20210A variant: prevalence in a U.K. anticoagulant clinic population
1997 • 172 citations
A Common Mutation in the Methylenetetrahydrofolate Reductase Gene (C677T) Increases the Risk for Deep-Vein Thrombosis in Patients With Mutant Factor V (Factor V:Q 506 )
1997 • 171 citations
The Heterozygous 20210 G/A Prothrombin Genotype Is Associated With Early Venous Thrombosis in Inherited Thrombophilias and Is Not Increased in Frequency in Artery Disease
1997 • 170 citations
Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3′‐untranslated region of the prothrombin gene
1997 • 160 citations
Thermolabile Methylenetetrahydrofolate Reductase and Factor V Leiden in the Risk of Deep-Vein Thrombosis
1998 • 160 citations
Factor V Leiden: An Additional Risk Factor for Thrombosis in Protein S Deficient Families?
1995 • 152 citations
A Single Genetic Origin for the Common Prothrombotic G20210A Polymorphism in the Prothrombin Gene
1998 • 147 citations
Hyperhomocysteinemia and Deep-Vein Thrombosis A Case-Control Study
1996 • 131 citations
Variability of Thrombosis among Homozygous Siblings with Resistance to Activated Protein C Due to an Arg-to-Gln Mutation in the Gene for Factor V
1994 • 125 citations
The Relative Frequency of Hereditary Thrombotic Disorders Among 107 Patients with Thrombophilia in Israel
1989 • 106 citations
Familial thrombophilia: a complex genetic disorder.
1997 • 101 citations
The first mutation identified in the thrombomodulin gene in a 45-year- old man presenting with thromboembolic disease
1995 • 95 citations
A Prothrombin Gene Mutation Is Significantly Associated With Venous Thrombosis
1997 • 83 citations
The VITA Project: C677T mutation in the methylene‐tetrahydrofolate reductase gene and risk of venous thromboembolism
1997 • 81 citations
Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficient newborn with massive thrombosis
1996 • 67 citations
The factor VR506Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis
1997 • 57 citations
The Prothrombin Gene 3′-Untranslated Region Mutation Is Frequently Associated With Factor V Leiden in Thrombophilic Patients and Shows Ethnic-Specific Variation in Allele Frequency
1998 • 38 citations
The G1691A mutation of the coagulation factor V gene (factor V Leiden) is rare in Chinese: an analysis of 618 individuals
1996 • 33 citations
Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Japanese patients with various forms of thrombosis, and normal individuals.
1996 • 32 citations
The Prothrombin Gene 3′-Untranslated Region Mutation Is Frequently Associated With Factor V Leiden in Thrombophilic Patients and Shows Ethnic-Specific Variation in Allele Frequency
1998 • 27 citations
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